Rao Sowmya, B T Nandish, Preman Namitha K, Johnson Renjith P, Ginjupalli Kishore, P Preethishree, Prabhu Ashwini, Das Ranajit, K Jayaprakash, Pai Vidya
Department of Dental Materials, Yenepoya Dental College, Yenepoya (Deemed to Be University), Mangalore, 575018, Karnataka, India.
Polymer Nanobiomaterial Research Laboratory, Smart Materials and Device Division, Yenepoya Research Centre, Yenepoya (Deemed to Be University), Mangalore, 575018, Karnataka, India.
Heliyon. 2022 Aug 23;8(8):e10374. doi: 10.1016/j.heliyon.2022.e10374. eCollection 2022 Aug.
The present study aims to synthesize and characterize two quaternary ammonium (QAM) based monomers such as - dimethyl-hexadecyl-methacryloxyethyl-ammonium iodide (DHMAI) and 2-dimethyl-2-dodecyl-1-methacryloxyethyl ammonium iodine (DDMAI) and assess their cytotoxicity and antimicrobial properties. The study also aims to incorporate the optimized concentration of these monomers as copolymerizing monomers into conventional Polymethyl methacrylate (PMMA) denture base resin and evaluate their suitability for prosthetic applications. DHMAI and DDMAI monomers were synthesized through a Menschutkin reaction and their chemical structure was characterized using FT-IR and H-NMR spectroscopy. Cytotoxicity was determined using Methyl Thiazolyl Tetrazolium (MTT) assay whereas antimicrobial activity was assessed using the agar-disc diffusion method. Subsequently, optimized concentrations of DHMAI or DDMAI, based on the cytotoxicity results, were added to conventional PMMA resin. Antimicrobial activity, cytotoxicity, surface hardness, and water sorption of PMMA denture base rein incorporated with DHMAI or DDMAI were evaluated. FT-IR and H-NMR results confirmed the structure of monomers and copolymerization of DHMAI and DDMAI with PMMA resin. DHMAI and DDMAI monomers were found to be cytocompatible with mouse fibroblast cells up to a concentration of 5 μg/mL and 20 μg/mL respectively. In addition, incorporation of DHMAI or DDMAI at 5 μg/mL and 20 μg/mL respectively into PMMA denture base material did not affect their cytocompatibility. PMMA denture base resin incorporated with DHMAI or DDMAI significantly reduced the adhesion of microbes. Further, an increase in the surface hardness and a reduction in the water sorption was observed. Hence DHMAI and DDMAI can be considered as potential candidates for imparting antimicrobial activity to polymeric denture base materials.
本研究旨在合成并表征两种基于季铵盐(QAM)的单体,即甲基丙烯酰氧乙基十六烷基二甲基碘化铵(DHMAI)和甲基丙烯酰氧乙基十二烷基二甲基碘化铵(DDMAI),并评估它们的细胞毒性和抗菌性能。该研究还旨在将这些单体的优化浓度作为共聚单体掺入传统的聚甲基丙烯酸甲酯(PMMA)义齿基托树脂中,并评估它们在修复应用中的适用性。通过门舒特金反应合成了DHMAI和DDMAI单体,并使用傅里叶变换红外光谱(FT-IR)和氢核磁共振光谱(H-NMR)对其化学结构进行了表征。使用甲基噻唑基四氮唑(MTT)法测定细胞毒性,而使用琼脂圆盘扩散法评估抗菌活性。随后,根据细胞毒性结果,将优化浓度的DHMAI或DDMAI添加到传统的PMMA树脂中。评估了掺入DHMAI或DDMAI的PMMA义齿基托树脂的抗菌活性、细胞毒性、表面硬度和吸水性。FT-IR和H-NMR结果证实了单体的结构以及DHMAI和DDMAI与PMMA树脂的共聚。发现DHMAI和DDMAI单体分别在浓度高达5μg/mL和20μg/mL时与小鼠成纤维细胞具有细胞相容性。此外,分别将5μg/mL和20μg/mL的DHMAI或DDMAI掺入PMMA义齿基托材料中不会影响其细胞相容性。掺入DHMAI或DDMAI的PMMA义齿基托树脂显著降低了微生物的粘附。此外,观察到表面硬度增加,吸水性降低。因此,DHMAI和DDMAI可被视为赋予聚合物义齿基托材料抗菌活性的潜在候选物。